a Department of Internal Medicine , Division of Cardiovascular Medicine, University of Iowa, Carver College of Medicine , Iowa City , IA , USA.
b Department of Cancer Biology and Genetics , The Ohio State University , Columbus , OH , USA.
Channels (Austin). 2017 Nov 2;11(6):673-677. doi: 10.1080/19336950.2017.1373225. Epub 2017 Oct 5.
Obesity is associated with a loss of insulin-sensitivity and systemic dysglycemia, resulting in Type 2 diabetes, however the molecular mechanisms underlying this association are unclear. Through adipocyte patch-clamp studies, we recently showed that SWELL1 is required for the Volume-Regulated Anion Current (VRAC) in adipocytes and that SWELL1-mediated VRAC is activated by both mechanical and pathophysiological adipocyte expansion. We also demonstrated that adipocyte SWELL1 is required for maintaining insulin signaling and glucose homeostasis, particularly in the setting of obesity. Here we show that SWELL1 protein expression is induced in subcutaneous fat, visceral fat and liver in the setting of obesity. Long- term AAV/rec2-shRNA mediated SWELL1 knock-down in both fat and liver are associated with increased weight gain, increased adiposity and exacerbated insulin resistance in mice raised on a high-fat diet. These data further support the notion that SWELL1 induction occurs in insulin- sensitive tissues (liver and adipose) in the setting of over-nutrition and contributes to improved systemic glycemia by supporting enhanced insulin-sensitivity.
肥胖与胰岛素敏感性丧失和全身血糖异常有关,导致 2 型糖尿病,但这种关联的分子机制尚不清楚。通过脂肪细胞膜片钳研究,我们最近表明,SWELL1 是脂肪细胞体积调节阴离子电流(VRAC)所必需的,并且 SWELL1 介导的 VRAC 可被机械和病理生理脂肪细胞扩张激活。我们还证明,脂肪细胞中的 SWELL1 对于维持胰岛素信号和葡萄糖稳态是必需的,特别是在肥胖的情况下。在这里,我们表明肥胖时,皮下脂肪、内脏脂肪和肝脏中的 SWELL1 蛋白表达增加。长期 AAV/rec2-shRNA 介导的脂肪和肝脏中的 SWELL1 敲低与高脂肪饮食喂养的小鼠体重增加、脂肪增多和胰岛素抵抗加重有关。这些数据进一步支持了这样一种观点,即过度营养时,胰岛素敏感组织(肝脏和脂肪组织)中会诱导 SWELL1 的表达,并通过支持增强的胰岛素敏感性来改善全身血糖。